Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs796051880
rs796051880
1 1.000 0.160 11 89191284 missense variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs104894314
rs104894314
8 0.790 0.160 11 89191205 missense variant G/A;T snv 8.0E-06; 9.2E-05 0.010 1.000 1 2001 2001